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Ciprofloxacin hydrochloride - 53808-0223-1 - (Ciprofloxacin hydrochloride)

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Drug Information of Ciprofloxacin hydrochloride

Product NDC: 53808-0223
Proprietary Name: Ciprofloxacin hydrochloride
Non Proprietary Name: Ciprofloxacin hydrochloride
Active Ingredient(s): 500    mg/1 & nbsp;   Ciprofloxacin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin hydrochloride

Product NDC: 53808-0223
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076089
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Ciprofloxacin hydrochloride

Package NDC: 53808-0223-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0223-1)

NDC Information of Ciprofloxacin hydrochloride

NDC Code 53808-0223-1
Proprietary Name Ciprofloxacin hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (53808-0223-1)
Product NDC 53808-0223
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin hydrochloride


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